NCT06503653进行中（未招募）不适用
Creation of a Syncope Channel for Patients Admitted to the Emergency Department for Loss of Consciousness and Not Hospitalized: Etiological Predictivity (Before/After Study)
Versailles Hospital2 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2024年3月31日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 52
- 试验地点
- 2
- 主要终点
- etiological diagnosis of synchope
研究概览
简要总结
The main aim of this study is to assess the value of creating a "syncope pathway" to optimize diagnostic performance in patients admitted to the emergency department for syncope and not hospitalized, compared with the previous pre-syncope pathway situation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Sequential
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults aged 18 and over;
- •Consultant at the emergency department of the Centre Hospitalier de V ersailles
- •For a confirmed diagnosis:
- •of recurrent syncope with low-risk criteria according to ESC 2018 (1,2) Or
- •of syncope recurrent or not, not fulfilling low-risk or high-risk criteria according to the ESC 2018 definition (1,2). These patients are those with minor high-risk criteria without aggravating circumstances:
- •With no personal history of loss of consciousness whose clinical features strongly suggest syncope of rhythmic origin;
- •No structural heart disease or abnormal ECG.
- •Outpatient (returning home after emergency);
- •Beneficiary or beneficiary of a social security scheme (excluding AME).
排除标准
- •Etiology of syncope identified as early as the emergency department visit;
- •High-risk syncope according to ESC 2018 criteria (1,3);
- •First and only episode of low-risk syncope according to ESC 2018 criteria (1,3);
- •Syncope of any risk category requiring hospitalization at the discretion of the emergency physician and cardiologist;
- •Legal protection by guardianship ;
- •Language barrier or condition incompatible with the patient's understanding or informed adherence to the protocol;
- •Opposition to the use of their pseudonymized data (for retrospective inclusions);
- •Patient's refusal to give consent to participate in the study (for prospective inclusions);
结局指标
主要结局
etiological diagnosis of synchope
时间窗: 3 months
Percentage of patients for whom at least one etiological diagnosis of syncope was identified.
次要结局
未报告次要终点
研究者
Dr laura Eouzan dahan
coordonator investigator
Versailles Hospital
研究点 (2)
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